Zhejiang Key Laboratory of Pathophysiology, Health Center, Ningbo University, Ningbo, Zhejiang, China.
Department of Psychiatry, Affiliated Kangning Hospital of Ningbo University, Ningbo, Zhejiang, China.
Br J Pharmacol. 2024 Jul;181(13):1952-1972. doi: 10.1111/bph.16319. Epub 2024 Mar 4.
In major depressive disorder (MDD), exploration of biomarkers will be helpful in diagnosing the disorder as well as in choosing a treatment and predicting the treatment response. Currently, tRNA-derived small ribonucleic acids (tsRNAs) have been established as promising non-invasive biomarker candidates that may enable a more reliable diagnosis or monitoring of various diseases. Herein, we aimed to explore tsRNA expression together with functional activities in MDD development.
Serum samples were obtained from patients with MDD and healthy controls, and small RNA sequencing (RNA-Seq) was used to profile tsRNA expression. Dysregulated tsRNAs in MDD were validated by quantitative real-time polymerase chain reaction (qRT-PCR). The diagnostic utility of specific tsRNAs and the expression of these tsRNAs after antidepressant treatment were analysed.
In total, 38 tsRNAs were significantly differentially expressed in MDD samples relative to healthy individuals (34 up-regulated and 4 down-regulated). qRT-PCR was used to validate the expression of six tsRNAs that were up-regulated in MDD (tiRNA-1:20-chrM.Ser-GCT, tiRNA-1:33-Gly-GCC-1, tRF-1:22-chrM.Ser-GCT, tRF-1:31-Ala-AGC-4-M6, tRF-1:31-Pro-TGG-2 and tRF-1:32-chrM.Gln-TTG). Interestingly, serum tiRNA-Gly-GCC-001 levels exhibited an area under the ROC curve of 0.844. Moreover, tiRNA-Gly-GCC-001 is predicted to suppress brain-derived neurotrophic factor (BDNF) expression. Furthermore, significant tiRNA-Gly-GCC-001 down-regulation was evident following an 8-week treatment course and served as a promising baseline predictor of patient response to antidepressant therapy.
Our current work reports for the first time that tiRNA-Gly-GCC-001 is a promising MDD biomarker candidate that can predict patient responses to antidepressant therapy.
在重度抑郁症(MDD)中,探索生物标志物将有助于诊断该疾病,以及选择治疗方法和预测治疗反应。目前,tRNA 衍生的小 RNA(tsRNAs)已被确立为很有前途的非侵入性生物标志物候选物,可实现对各种疾病的更可靠诊断或监测。在此,我们旨在探索 tsRNA 表达及其在 MDD 发展中的功能活动。
从 MDD 患者和健康对照者中获得血清样本,并进行小 RNA 测序(RNA-Seq)以分析 tsRNA 表达谱。采用定量实时聚合酶链反应(qRT-PCR)验证 MDD 中失调的 tsRNAs。分析特定 tsRNA 的诊断效用以及抗抑郁治疗后这些 tsRNA 的表达。
MDD 样本中共有 38 个 tsRNA 与健康个体相比存在显著差异表达(34 个上调,4 个下调)。qRT-PCR 用于验证在 MDD 中上调的 6 个 tsRNA 的表达(tiRNA-1:20-chrM.Ser-GCT、tiRNA-1:33-Gly-GCC-1、tRF-1:22-chrM.Ser-GCT、tRF-1:31-Ala-AGC-4-M6、tRF-1:31-Pro-TGG-2 和 tRF-1:32-chrM.Gln-TTG)。有趣的是,血清 tiRNA-Gly-GCC-001 水平的 ROC 曲线下面积为 0.844。此外,预测 tiRNA-Gly-GCC-001 可抑制脑源性神经营养因子(BDNF)的表达。此外,在 8 周的治疗过程中,tiRNA-Gly-GCC-001 明显下调,作为抗抑郁治疗患者反应的有前途的基线预测因子。
我们的研究首次报道 tiRNA-Gly-GCC-001 是 MDD 的有前途的生物标志物候选物,可预测患者对抗抑郁治疗的反应。